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Quality of Medicines in Portugal: A Retrospective Review of Medicine Recalls (2000–2015)

机译:葡萄牙药物的质量:医学召回的回顾性审查(2000-2015)

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摘要

INFARMED, the Portuguese national health authority, alerts the general public and health care professionals about quality or safety issues detected in health products. The present study analyses recalls of substandard medicines in Portugal between 2005 and 2015. All 338 alerts for medicine recalls were analysed, which represents a total of 378 drugs withdrawn. Despite the fact that the total number of medicine alerts has increased during the past decade, the number of actual medicine recalls remained relatively constant. The number of batches affected in each recall varies from only one to several batches. In addition, 294 of the alerts are related to voluntary recalls, that is, those initiated by the marketing authorisation holder, whereas only 40 were mandatory recalls. There are marketing authorisation holders that have had several medicine recalls over the period studied. The main cause of product recall was the pharmaceutical dosage form, followed by packaging problems. Forty-two percent of the withdrawn medicines are from solid oral forms, a value slightly higher than that obtained for the injectables group. Finally, substandard medicines have been accessible in the Portuguese market for a period that varied between one month and over four years. The data seem to show that the number of substandard medicines in Portugal has not been increasing. However, this may be due to a variety of causes, that is, better performance of the industry, non-detection of these cases, and so on.
机译:葡萄牙国家卫生管理局挤压,警告一般公众和医疗保健专业人员关于在卫生产品中检测到的质量或安全问题。本研究分析了2005年至2015年葡萄牙不合标准的药物回忆。分析了所有338份药物召回警报,其中占撤出了378种药物。尽管过去十年中的药物警报总数增加,但实际药物的数量召回仍然相对恒定。在每个召回中受影响的批次数量从一个到几个批次不同。此外,警报294与自愿召回有关,即由营销授权持有人发起的人,而只有40个是强制性的召回。在研究期间,有几种药物召回的营销授权持有人。产品召回的主要原因是药物剂型,其次是包装问题。四十二百分之一的撤出药物来自固体口服形式,值略高于注射物组的值。最后,葡萄牙市场的不合标准药物可在一个月间和四年之间变化的时期。这些数据似乎表明葡萄牙的不合标准药物数量尚未增加。但是,这可能是由于各种原因,即,更好地表现行业,无检测这些情况,等等。

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